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SMILES: Oc1ccc(CCCCCC(=O)N2CCOC2=O)cc1

InChI Key: InChIKey=DHWUVTVUAVGPBO-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 319818   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kcal/mole	IC50 nM	Kd nM	EC50/IC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
N-acylethanolamine-hydrolyzing acid amidase (Homo sapiens (Human))	BDBM319818 (US10174015, Compound 31) Show SMILES Oc1ccc(CCCCCC(=O)N2CCOC2=O)cc1 Show InChI InChI=1S/C15H19NO4/c17-13-8-6-12(7-9-13)4-2-1-3-5-14(18)16-10-11-20-15(16)19/h6-9,17H,1-5,10-11H2	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	90	n/a	n/a	n/a	n/a	n/a	n/a
Xiamen University US Patent					Assay Description In the Experimental example, endocannabinoid hydrolases used were Fatty Acid Amide Hydrolase (FAAH) and N-acylethanolamide hydrolyzing acid amidase (...				US Patent US10174015 (2019) BindingDB Entry DOI: 10.7270/Q2M047JS
					More data for this Ligand-Target Pair
N-acylethanolamine-hydrolyzing acid amidase (Rattus norvegicus (Rat))	BDBM319818 (US10174015, Compound 31) Show SMILES Oc1ccc(CCCCCC(=O)N2CCOC2=O)cc1 Show InChI InChI=1S/C15H19NO4/c17-13-8-6-12(7-9-13)4-2-1-3-5-14(18)16-10-11-20-15(16)19/h6-9,17H,1-5,10-11H2	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	61	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Sciences Curated by ChEMBL					Assay Description Inhibition of rat NAAA expressed in HEK293 cells using heptadecenoylethanolamide as substrate after 30 mins by HPLC-MS/MS analysis				Eur J Med Chem 139: 214-221 (2017) Article DOI: 10.1016/j.ejmech.2017.08.004 BindingDB Entry DOI: 10.7270/Q2FR007C
					More data for this Ligand-Target Pair
Acid ceramidase (Rattus norvegicus (Rat))	BDBM319818 (US10174015, Compound 31) Show SMILES Oc1ccc(CCCCCC(=O)N2CCOC2=O)cc1 Show InChI InChI=1S/C15H19NO4/c17-13-8-6-12(7-9-13)4-2-1-3-5-14(18)16-10-11-20-15(16)19/h6-9,17H,1-5,10-11H2	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	61	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Sciences Curated by ChEMBL					Assay Description Inhibition of rat acid ceramidase expressed in HEK293 cells using N-lauroylceramide as substrate after 30 mins by LC-MS analysis				Eur J Med Chem 139: 214-221 (2017) Article DOI: 10.1016/j.ejmech.2017.08.004 BindingDB Entry DOI: 10.7270/Q2FR007C
					More data for this Ligand-Target Pair
Fatty-acid amide hydrolase 1 (Homo sapiens (Human))	BDBM319818 (US10174015, Compound 31) Show SMILES Oc1ccc(CCCCCC(=O)N2CCOC2=O)cc1 Show InChI InChI=1S/C15H19NO4/c17-13-8-6-12(7-9-13)4-2-1-3-5-14(18)16-10-11-20-15(16)19/h6-9,17H,1-5,10-11H2	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	260	n/a	n/a	n/a	n/a	n/a	n/a
Xiamen University US Patent					Assay Description In the Experimental example, endocannabinoid hydrolases used were Fatty Acid Amide Hydrolase (FAAH) and N-acylethanolamide hydrolyzing acid amidase (...				US Patent US10174015 (2019) BindingDB Entry DOI: 10.7270/Q2M047JS
					More data for this Ligand-Target Pair